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Chromatin Modification in iPS Cells01:32

Chromatin Modification in iPS Cells

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Chromatin modification alters gene expression; therefore, scientists can add histone-modifying enzymes, histone variants, and chromatin remodeling complexes to somatic cells to aid reprogramming into pluripotent stem (iPS) cells.
Compact chromatin makes reprogramming difficult. Enzymes, such as histone demethylases and acetyltransferases, are often added during reprogramming to loosen the chromatin, making the DNA more accessible to transcription factors. Molecules that inhibit histone...
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Methods of Nuclear Reprogramming01:24

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Nuclear reprogramming is a process of transforming one cell type into an unrelated cell type by epigenetic changes that alter the cell’s original gene expression pattern. Such epigenetic changes force cells to express a different set of genes, which play a significant role in inducing transformation into other cell types. Nuclear reprogramming offers applications in reproductive cloning for livestock propagation and regenerative medicine — developing patient-specific cells for...
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Somatic to iPS Cell Reprogramming01:29

Somatic to iPS Cell Reprogramming

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Reprogramming alters the gene expression in somatic cells, transforming them into induced pluripotent stem (iPS) cells over several generations. Scientists can reprogram cells by introducing genes for four transcription factors—Oct4, Sox2, Klf4, and c-Myc (OSKM) by viral or non-viral methods. These factors are also known as Yamanaka factors after Shinya Yamanaka, who first generated iPS cells using mouse skin cells. Yamanaka was awarded the Nobel Prize in Physiology or Medicine in 2012...
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Introduction to Nuclear Reprogramming01:14

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Nuclear reprogramming is the process of switching gene expression of one cell type to that of another cell type, usually from a differentiated cell state to an undifferentiated cell state. Differentiation occurs during processes such as development and morphogenesis, tissue regeneration, and malignancy. Cells can also be artificially induced to reprogram their gene expression by techniques such as nuclear transfer, induced pluripotency, and cell fusion. Such techniques have many applications in...
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Duplication of Chromatin Structure02:05

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The process of chromosome duplication during cell division requires genome-wide disruption and re-assembly of chromatin. The chromatin structure must be accurately inherited, reassembled, and maintained in the daughter cells to ensure lineage propagation.
The basic unit of the chromatin is the nucleosome, consisting of DNA wrapped around octameric histone proteins and short stretches of linker DNA separating individual nucleosomes. The histone proteins within the nucleosome have their...
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Inheritance of Chromatin Structures03:17

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Epigenetics is the study of inherited changes in a cell's phenotype without changing the DNA sequences. It provides a form of memory for the differential gene expression pattern to maintain cell lineage, position-effect variegation, dosage compensation, and maintenance of chromatin structures such as telomeres and centromeres. For example, the structure and location of the centromere on chromosomes are epigenetically inherited. Its functionality is not dictated or ensured by the underlying...
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Video Experimental Relacionado

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Author Spotlight: Reprogramming Cancer Cells to iPSCs to Study Disease Progression and Treatment Targets
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Dinámica de la cromatina durante la reprogramación celular.

Effie Apostolou1, Konrad Hochedlinger

  • 11] Massachusetts General Hospital Center for Regenerative Medicine, 185 Cambridge Street, Boston, Massachusetts 02114, USA. [2] Harvard Stem Cell Institute, 1350 Masschusetts Avenue, Cambridge, Massachusetts 02138, USA. [3] Howard Hughes Medical Institute, 4000 Jones Bridge Road, Chevy Chase, Maryland 20815, USA. [4] Department of Stem Cell and Regenerative Biology, Harvard University and Harvard Medical School, 7 Divinity Avenue, Cambridge, Massachusetts 02138, USA.

Nature
|October 25, 2013
PubMed
Resumen
Este resumen es generado por máquina.

La pluripotencia inducida genera células madre específicas del paciente y revela información sobre los factores de transcripción y la estructura de la cromatina. El estudio de estas dinámicas puede avanzar en la medicina regenerativa y las terapias contra el cáncer.

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Área de la Ciencia:

  • * Biología de las células madre y epigenética.
  • * Mecanismos moleculares de la determinación del destino celular.

Sus antecedentes:

  • * La tecnología de pluripotencia inducida (iPSC) permite la generación de células madre específicas del paciente.
  • * La tecnología iPSC ofrece un modelo para estudiar las interacciones entre el factor de transcripción y la cromatina.
  • * Comprender la dinámica de la cromatina es crucial para las transiciones de estado celular.

Objetivo del estudio:

  • * Revisar los avances recientes en la dinámica de la cromatina durante la pluripotencia inducida.
  • * Para comparar los eventos de cromatina de iPSC con la maduración de las células germinales y la tumorigénesis.
  • * Explorar aplicaciones potenciales en medicina regenerativa y tratamiento del cáncer.

Principales métodos:

  • * Revisión de la literatura actual sobre la pluripotencia inducida y la dinámica de la cromatina.
  • * Análisis comparativo de la remodelación de la cromatina en las células iPSC, las células germinales y los tumores.
  • * Síntesis de los hallazgos para proponer ideas mecanicistas integradas.

Principales resultados:

  • * La cromatina sufre cambios dinámicos significativos durante la inducción de la pluripotencia.
  • * Existen similitudes en los procesos de remodelación de la cromatina a través de la pluripotencia, el desarrollo de células germinales y el cáncer.
  • * Estos eventos dinámicos de la cromatina son clave para regular el destino celular.

Conclusiones:

  • * La pluripotencia inducida proporciona un marco valioso para el estudio de la biología celular fundamental.
  • * Una visión integrada de la dinámica de la cromatina en diversos procesos puede dar lugar a nuevas estrategias terapéuticas.
  • * Investigaciones adicionales pueden desbloquear nuevos enfoques de medicina regenerativa y tratamiento del cáncer.